ClinVar Miner

Submissions for variant NM_004992.3(MECP2):c.*9G>A (rs144008995)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000153483 SCV000202999 benign not specified 2014-01-08 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000153483 SCV000595743 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV000719347 SCV000850213 benign History of neurodevelopmental disorder 2013-12-29 criteria provided, single submitter clinical testing
RettBASE RCV000153483 SCV000187799 benign not specified 2010-08-24 no assertion criteria provided curation

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